Allele Registry

Canonical Allele Identifier: PA2825229354

Gene: RARB HGNC NCBI

ClinVar RCV:

RCV001089954

ClinVar Variation:

870386

HGVS (amino-acid)	Matching Registered Transcripts
NP_000956.2:p.Phe279Val	CA351886271 NM_000965.5:c.835T>G